Canonical Allele Identifier: CA1012887455
Gene: TMEM63A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225852481_225852484dup , CM000663.2:g.225852481_225852484dup GRCh38
NC_000001.10:g.226040182_226040185dup , CM000663.1:g.226040182_226040185dup GRCh37
NC_000001.9:g.224106805_224106808dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366835.8:c.1903+180_1903+183dup MANE Select ENSP00000355800.3:n.1903+180_1903+183dup
ENST00000366835.7:c.1903+180_1903+183dup ENSP00000355800.3:n.1903+180_1903+183dup
NM_014698.2:c.1903+180_1903+183dup NP_055513.2:n.1903+180_1903+183dup
XM_006711841.2:c.1372+180_1372+183dup XP_006711904.1:n.1372+180_1372+183dup
XM_011544328.1:c.1903+180_1903+183dup XP_011542630.1:n.1903+180_1903+183dup
XM_011544329.1:c.1903+180_1903+183dup XP_011542631.1:n.1903+180_1903+183dup
XM_011544330.1:c.1903+180_1903+183dup XP_011542632.1:n.1903+180_1903+183dup
XM_011544331.1:c.1816+180_1816+183dup XP_011542633.1:n.1816+180_1816+183dup
XM_011544332.1:c.1462+180_1462+183dup XP_011542634.1:n.1462+180_1462+183dup
XR_949163.1:n.2208+180_2208+183dup
XM_006711841.4:c.1372+180_1372+183dup XP_006711904.1:n.1372+180_1372+183dup
XM_011544328.3:c.1903+180_1903+183dup XP_011542630.1:n.1903+180_1903+183dup
XM_011544329.3:c.1903+180_1903+183dup XP_011542631.1:n.1903+180_1903+183dup
XM_011544330.3:c.1903+180_1903+183dup XP_011542632.1:n.1903+180_1903+183dup
XM_011544331.3:c.1816+180_1816+183dup XP_011542633.1:n.1816+180_1816+183dup
XM_011544332.3:c.1462+180_1462+183dup XP_011542634.1:n.1462+180_1462+183dup
XR_001737552.2:n.1990+180_1990+183dup
XR_949163.3:n.2187+180_2187+183dup
NM_014698.3:c.1903+180_1903+183dup MANE Select NP_055513.2:n.1903+180_1903+183dup